Evidence map›Paper›PMID 34164355›Full record

ArticleFrontiers in pediatrics2021

Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in

Benzhen Wang, Zhanhui Du, Guangsong Shan, Chuanzhu Yan, Victor Wei Zhang, Zipu Li

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.8field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Article
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  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Benzhen WangQingdao Women and Children's Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Zhanhui DuHeart Center, Qingdao Women and Children's Hospital, Affiliated to Qingdao University, Qingdao, China.
Guangsong ShanHeart Center, Qingdao Women and Children's Hospital, Affiliated to Qingdao University, Qingdao, China.
Chuanzhu YanDepartment of Neurology, Qilu Hospital of Shandong University, Jinan, China.
Victor Wei ZhangDepartment of Human and Molecular Genetics, Baylor College of Medicine, Houston, TX, United States.
Zipu LiHeart Center, Qingdao Women and Children's Hospital, Affiliated to Qingdao University, Qingdao, China.
Qingdao Women and Children's Hospital · CNBaylor College of Medicine · USQilu Hospital of Shandong University · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sengers syndrome (OMIM #212350) is a rare autosomal recessive disorder due to mutations in acylglycerol kinase (

Indexed as

acylglycerol kinasecardiomyopathygenotypehypertrophicmutationSengers syndrome

Identifiers

PMID34164355
PMCPMC8215120
OpenAlexW3166664645

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.